A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622890



Internal ID21814937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:192071..192071hg38UCSC Ensembl
chr18:192071..192071hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6111108
Supporting Variants
Samples
Known GenesUSP14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622890
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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